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FDA 510(k) Applications Submitted by ANGELA CARAVELLA
FDA 510(k) Number
Submission Date
Device Name
Applicant
K102194
08/04/2010
SOLCART B
B. BRAUN AVITUM AG
K100334
02/05/2010
DIACAP POLYSULFONE HIFLO 23 HEMODILAYZER , MODEL 72036811
B. BRAUN AVITUM AG
K090884
03/31/2009
PERIFIX ONE PEDIATRIC CATHETER, 20 GA. & 24 GA.
B. BRAUN MEDICAL, INC.
K090905
04/01/2009
ADDEASE 20MM BINARY CONNECTOR WITH 17 GA. NEEDLE
B. BRAUN MEDICAL, INC.
K140838
04/02/2014
IV ADMINISTRATION SET WITH HAND PUMP
B. BRAUN MEDICAL, INC.
K111236
05/02/2011
INTROCAN SAFETY (R) 3 CLOSED IV CATHETER 18GA X 1-3/4 (45MM) AND 18GA X 1-1/4 (32MM) / 20GA X 1-1/4 (32MM) / 20GA X 1
B. BRAUN MELSUNGEN AG
K112636
09/09/2011
CYTOGUARD(TM) CLOSED LUER CONNECTOR
B. BRAUN MEDICAL, INC.
K143082
10/27/2014
IV Administration Sets with 200(micro)m Blood Filter
B. Braun Medical Inc.
K170897
03/27/2017
Surecan Safety II Needle, Surecan Safety II Needle, Surecan Safety II Needle with Caresite Luer Access Device and Y site
B. Braun Medical Inc.
K201469
06/03/2020
Mini Spike Plus 6/8R
B. Braun Medical Inc.
K191658
06/21/2019
IV Sets not made with PVC
B. Braun Medical Inc.
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